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956578-85-1

C40H57N3O12 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 956578-85-1 Structure

  • Basic information

    1. Product Name: C40H57N3O12
    2. Synonyms: C40H57N3O12
    3. CAS NO:956578-85-1
    4. Molecular Formula:
    5. Molecular Weight: 771.905
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 956578-85-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: C40H57N3O12(CAS DataBase Reference)
    10. NIST Chemistry Reference: C40H57N3O12(956578-85-1)
    11. EPA Substance Registry System: C40H57N3O12(956578-85-1)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 956578-85-1(Hazardous Substances Data)

956578-85-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 956578-85-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,6,5,7 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 956578-85:
(8*9)+(7*5)+(6*6)+(5*5)+(4*7)+(3*8)+(2*8)+(1*5)=241
241 % 10 = 1
So 956578-85-1 is a valid CAS Registry Number.

956578-85-1Upstream product

956578-85-1Downstream Products

956578-85-1Relevant articles and documents

Synthesis of chlorogenic acid derivatives with promising antifungal activity

Ma, Chao-Mei,Kully, Maureen,Khan, Jehangir K.,Hattori, Masao,Daneshtalab, Mohsen

, p. 6830 - 6833 (2007)

Derivatives of chlorogenic acid or its analogues were synthesized by coupling protected chlorogenic acid or its analogues with p-octyloxyaniline and selected amino acids. Most of the compounds exhibited significant potency against Cryptococcus neoformans and Candida species with low toxicity to brine shrimps. The 4,5-dihydroxyl groups in the quinic acid moiety were necessary for the activity and introduction of a free amino group increased the inhibitory activity against Aspergillus fumigatus.

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